Label: HGH PLUS- alpha gpc, deer antler velvet, hepar suis, hgh, igf-1, igf-2, pituitarum post spray
- NDC Code(s): 43853-0028-1
- Packager: ProBlen
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved homeopathic
DISCLAIMER: This homeopathic product has not been evaluated by the Food and Drug Administration for safety or efficacy. FDA is not aware of scientific evidence to support homeopathy as effective.
Drug Label Information
Updated October 25, 2021
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WARNINGS
Warnings: Not for use on children. If symptoms continue to recur, or if sleeplessness persists continuously for more than two weeks, consult a physician. Insomnia may be a symptom of a serious underlying medical illness. As with all medicines, if you are pregnant or breast feeding, consult a health professional before using this product. Keep out of the reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.
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INGREDIENTS AND APPEARANCE
HGH PLUS
alpha gpc, deer antler velvet, hepar suis, hgh, igf-1, igf-2, pituitarum post sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:43853-0028 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALPHA (UNII: AC10C1L8VO) (ALPHA - UNII:AC10C1L8VO) ALPHA 8 [hp_X] in 30 mL CERVUS ELAPHUS VELVET (UNII: Z608183YD0) (CERVUS ELAPHUS VELVET - UNII:Z608183YD0) CERVUS ELAPHUS VELVET 6 [hp_X] in 30 mL PORK LIVER (UNII: 6EC706HI7F) (PORK LIVER - UNII:6EC706HI7F) PORK LIVER 6 [hp_X] in 30 mL SOMATROPIN (UNII: NQX9KB6PCL) (SOMATROPIN - UNII:NQX9KB6PCL) SOMATROPIN 12 [hp_X] in 30 mL DALOTUZUMAB (UNII: 6YI1L648RH) (DALOTUZUMAB - UNII:6YI1L648RH) DALOTUZUMAB 12 [hp_X] in 30 mL INSULIN-LIKE GROWTH FACTOR-2 (UNII: 95067D43FQ) (INSULIN-LIKE GROWTH FACTOR-2 - UNII:95067D43FQ) INSULIN-LIKE GROWTH FACTOR-2 12 [hp_X] in 30 mL SUS SCROFA PITUITARY GLAND, POSTERIOR (UNII: E8S87O660T) (SUS SCROFA PITUITARY GLAND, POSTERIOR - UNII:E8S87O660T) SUS SCROFA PITUITARY GLAND, POSTERIOR 5 [hp_C] in 30 mL Inactive Ingredients Ingredient Name Strength ALCOHOL (UNII: 3K9958V90M) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:43853-0028-1 30 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 05/09/2017 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 05/09/2017 Labeler - ProBlen (838787161)